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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 11,138 Chinese ancestry cases, 85,294 Chinese ancestry controls.
The effect
Each copy of the A allele carried 2.71 times the odds of Gestational thrombocytopenia (95% confidence interval 2.13-3.45); p = 4 × 10−16.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 1, band 1q23.1 — between genes, 3.2 kb from SMU1P1.
What each result means
A/ATwo copies of the version the research linked to Gestational thrombocytopenia. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Gestational thrombocytopenia. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Gestational thrombocytopenia. This is the starting point the study compared everyone against.
rs117246523 is a single position in the genome, in or near the near SMU1P1 gene. Published research associates it with gestational thrombocytopenia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117246523 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs117246523 come from?
GWAS Catalog, Blood 2024, PMID:38064665. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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